Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913527 | 0.807 | 0.320 | 12 | 25225628 | missense variant | C/A;G;T | snv | 6 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913527 | 0.807 | 0.320 | 12 | 25225628 | missense variant | C/A;G;T | snv | 6 |